scholarly journals Cmv-1, a genetic locus that controls murine cytomegalovirus replication in the spleen.

1990 ◽  
Vol 171 (5) ◽  
pp. 1469-1483 ◽  
Author(s):  
A A Scalzo ◽  
N A Fitzgerald ◽  
A Simmons ◽  
A B La Vista ◽  
G R Shellam

The genetic basis of the control of acute splenic MCMV infection was studied after intraperitoneal inoculation of the virus. Classical Mendelian analyses using C57BL/6 (resistant) and BALB/c (susceptible) parental strains disclosed an autosomal dominant non-H-2 gene that regulates splenic virus replication. The probable location of this gene, to which we have assigned the symbol Cmv-1, is on chromosome 6 as defined by the strain distribution pattern of splenic MCMV replication in CXB recombinant inbred mice. Although there is a similar hierarchy of resistance to MCMV and HSV-1 with respect to the C57BL and BALB genetic backgrounds, the strain distribution pattern of HSV-1 replication in recombinant inbred mice suggests that Cmv-1 is not involved in restricting the spread of this virus. This is the first clear identification of a non-H-2 gene regulating the magnitude of MCMV infection. Elucidation of the function of this gene may be a fundamental step towards understanding the control of systemic CMV infection.

1993 ◽  
Vol 4 (3) ◽  
pp. 148-152 ◽  
Author(s):  
Jian-Long Mu ◽  
J�rgen K. Naggert ◽  
Patsy M. Nishina ◽  
Yin-Chai Cheah ◽  
Beverly Paigen

1996 ◽  
Vol 7 (7) ◽  
pp. 526-532 ◽  
Author(s):  
K. L. Shultz ◽  
K. L. Svenson ◽  
Y. -C. Cheah ◽  
B. Paigen ◽  
W. G. Beamer

1995 ◽  
Vol 6 (12) ◽  
pp. 867-872 ◽  
Author(s):  
K. L. Svenson ◽  
Y. C. Cheah ◽  
K. L. Shultz ◽  
J. L. Mu ◽  
B. Paigen ◽  
...  

1983 ◽  
Vol 158 (5) ◽  
pp. 1693-1702 ◽  
Author(s):  
J E Silver ◽  
T N Fredrickson

The seven CXB recombinant inbred strains were tested for susceptibility to Friend helper virus (F-MuLV) hematopoietic neoplasms. BALB/c and CXB-H mice develop erythroblastosis after neonatal inoculation with F-MuLV, while C57BL/6 and the six other RI strains develop lymphoma and myelogenous leukemia. This strain distribution pattern is different from that for H-2, Gpd-1 (linked to Fv-1), Fv-2, Rfv-3, and Cv (linked to Rmcf) but the same as that for Bv, the endogenous ecotropic virus of C57BL/6. However, analysis of crosses segregating Bv show that resistance to F-MuLV erythroblastosis is not linked to Bv. Disease-free survival is shortest for BALB/c mice, intermediate for CXB-H and CXB-J, and longest for C57BL/6 and the other RI strains. We conclude: (a) the major C57BL/6 gene for resistance to F-MuLV erythroblastosis is different from previously identified Friend virus restriction loci; (b) latency for F-MuLV leukemias is controlled by more than one gene; and (c) latency and susceptibility to F-MuLV erythroblastosis are not inherited concordantly in the CXB-RI strains.


Biomolecules ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 1762
Author(s):  
Airton C. Martins ◽  
Caridad López-Granero ◽  
Beatriz Ferrer ◽  
Alexey A. Tinkov ◽  
Anatoly V. Skalny ◽  
...  

BXD recombinant inbred (RI) lines represent a genetic reference population derived from a cross between C57BL/6J mice (B6) and DBA/2J mice (D2), which through meiotic recombination events possesses recombinant chromosomes containing B6 or D2 haplotype segments. The quantitative trait loci (QTLs) are the locations of segregating genetic polymorphisms and are fundamental to understanding genetic diversity in human disease susceptibility and severity. QTL mapping represents the typical approach for identifying naturally occurring polymorphisms that influence complex phenotypes. In this process, genotypic values at markers of known genomic locations are associated with phenotypic values measured in a segregating population. Indeed, BXD RI strains provide a powerful tool to study neurotoxicity induced by different substances. In this review, we describe the use of BXD RI lines to understand the underlying mechanisms of neurotoxicity in response to ethanol and cocaine, as well as metals and pesticide exposures.


1990 ◽  
Vol 27 (5) ◽  
pp. 362-364 ◽  
Author(s):  
P. F. Frelier ◽  
J. W. Templeton ◽  
M. Estes ◽  
H. W. Whitford ◽  
R. D. Kienle

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